CRANFIELD UNIVERSITY Eleni Anthippi Chatzimichali ...

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1 Introduction and Literature Review 1.1 Introduction 1.1.1 Overview of Systems Biology Breakthrough biological discoveries over the past decades, such as the revolutionary discovery of the double helix structure of DNA in 1953 by Watson and Crick, catalysed the blossoming of molecular biology (Watson and Crick, 1953). Acquiring information about the structure and properties of DNA and proteins led to outstanding progress in the years that followed as presented in Figure 1-1. Molecular biology has chiefly focused on identifying and investigating individual biological molecules by studying their properties and functions either as isolated entities or as small sets of components in very simple model systems. However, the reductionist approach adapted by molecular biology was not sufficient to interpret the intrinsic complexity of biological systems. The Human Genome Project has profoundly altered the practice and view of contemporary biology (Hood, 2003; Venter et al., 2001). In the post-genome era, the massive amount of biological data acquired by the advance of high-throughput technologies led to the rapid shift of interest towards systems biology. The marked increase in the amount of genomic, proteomic and metabolomic data due to the constant improvements in high-throughput tools, has granted the scientific community the opportunity to study complex biological systems as an integrated whole. Thus, systems biology emerged as a necessity helping us understand these complex system dynamics, as these are the key to understanding life. Systems analysis has historically been applied in a plethora of scientific fields such as economics, physics, psychology and most recently biology, covering a multitude of different areas such as developmental biology, ecology and immunology (Westerhoff et al., 2004). 1
Figure 1-1 Evolution from molecular biology to systems biology The line of inquiry represents the way mainstream molecular biology, under the pressure for systemlevel study, started investigating groups of molecules rather than single macromolecules, while simultaneously investigated their interactions. The figure has been adapted from Westhoff et al. (2004). A system-level approach aims to generate novel technologies and effective tools based on the collection, integration, analysis, graphical visualisation, and ultimately modelling of biological information (Ideker et al., 2001; Hood, 2003). Mathematical modelling is the backbone of contemporary systems biology. To this day the term “mathematical” is usually hidden behind a “computational approach” (Mesarovic et al., 2005). A model is an effort to represent all the integrated highly heterogeneous information that derives from multiple experimental sources in an abstract manner. Current advances in systems biology and computing science are prompting scientists to use sophisticated mathematical models and powerful in silico simulations. Despite the continuous acquisition of new information as well as the overwhelming progress of computational and experimental methods, the high complexity of biological systems will always constitute an obstacle for the construction of a general, integrated and functionally meaningful model based on complete understanding (Butcher et al., 2004; Filkenstein et al., 2004). 2
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Page 3 and 4: ABSTRACT Muscle foods such as meat,
Page 5 and 6: TABLE OF CONTENTS ABSTRACT ........
Page 7 and 8: 6.2.4 The iWebPlots package .......
Page 9 and 10: Figure 3-12 Speedup produced by the
Page 11 and 12: Figure 6-9 Sweave example for the d
Page 13 and 14: TABLE OF EQUATIONS Equation 1 Mean-
Page 15: RMSE RMSECV SSE SVD SVMs SYMBIOSIS-
Page 19 and 20: 1.1.2.1 Fourier Transform Infrared
Page 21 and 22: 1.1.3 Microbial Spoilage in Meat Sy
Page 23 and 24: The multivariate techniques applied
Page 25 and 26: 1.4 Multivariate Analysis: Unsuperv
Page 27 and 28: 1.4.2 Cluster Analysis Cluster anal
Page 29 and 30: 1.5 Multivariate Analysis: Supervis
Page 31 and 32: In any linearly separable binary da
Page 33 and 34: Where ( ) are the Lagrange multipli
Page 35 and 36: Every kernel is characterised by a
Page 37 and 38: The “one-against-all” approach
Page 39 and 40: Furthermore, metrics such as the bi
Page 41 and 42: 1.6.3 Leave-One-Out Cross-Validatio
Page 43 and 44: In such cases, the model becomes qu
Page 45 and 46: 1.8 Aims and objectives The overall
Page 47 and 48: 2 Development of the multivariate a
Page 49 and 50: Sensory panel scores were of the hi
Page 51 and 52: DF (Hz) 2.2.1.5 Electronic Nose (e-
Page 53 and 54: Figure 2-3 Data intersection The fi
Page 55 and 56: 3. Validation Techniques In the cas
Page 57 and 58: Figure 2-4 The process of construct
Page 59 and 60: 2.3 Results and Discussion 2.3.1 Pr
Page 61 and 62: (b) HPLC data (c) e-nose data Figur
Page 63 and 64: In the case of FTIR, linear classif
Page 65 and 66: 2.3.2.2 Class Prediction Accuracies
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Figure 2-7 Class prediction rates o
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The topology of the three-dimension
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Figure 2-9 Three-dimensional error
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Furthermore, a thorough comparison
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In the master/slave architecture, a
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precision of the classification acc
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Figure 3-3 The steps of the Nelder-
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3.3 Results and Discussion 3.3.1 Li
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3.3.2 Nonlinear Models In order to
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9) 10) 11) 12) 13) 14) 15) 16) Figu
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As an additional visual aid, these
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a) Number of iterations b) Number o
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Figure 3-10 Comparison of the execu
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Figure 3-12 Speedup produced by the
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4 Integration of Heterogeneous Data
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4.2.2 Procrustes Analysis Procruste
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symmetric method since the ordering
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Figure 4-3 Steps of CPCA for the da
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4.2.5 Data Integration and Analysis
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Figure 4-4 Data integration workflo
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a) GPA b) CPCA Figure 4-6 The conse
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accuracies as the linear models; po
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Figure 4-8 Classification Results f
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Similar to FTIR, the PLS-DA ensembl
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4.3.3 Permutation Tests Even though
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Even though the interpretation of t
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Figure 4-12 Distribution plots of t
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RBF SVMs Datasets Original %CC Mean
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Figure 4-14 Boxplots representing t
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5 Application of the multivariate a
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Figure 5-1 Mean FTIR spectra for ca
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5.2.2.2 Fourier Transform Infrared
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5.2.2.4 Data Overview For each expe
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5.2.3.3 High Throughput Liquid Chro
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Figure 5-5 displays the PCA scores
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(a) GPA (b) CPCA Figure 5-6 The con
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observation confirms that indeed CP
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(a) RBF SVMs (b) PLS-DA Figure 5-9
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Figure 5-12 Execution times of the
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(a) FTIR data (b) Raman data Figure
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The classification results for the
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Figure 5-16 Class prediction rates
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(a) RBF SVMs (b) PLS-DA Figure 5-17
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Figure 5-20 Execution times of the
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(a) FTIR data (b) HPLC data 148
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(a) GPA (b) CPCA Figure 5-22 The co
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The classification results of the f
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Figure 5-24 Classification Results
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Figure 5-25 Class prediction rates
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The permutation results for the dat
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Figure 5-28 Distribution plots of t
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Figure 5-30 Boxplots representing t
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5.4 Comparison of the individual ca
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Figure 5-32 Investigating the commo
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6 Development of improved visualisa
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6.2.2 Generating static graphs As d
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Figure 6-2 Construction process of
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6.2.2.2 Generating dynamic reports
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activity, while simultaneously the
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or disappeared (Wang et al., 2008).
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ectangles, circles and/or irregular
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In addition to the static figures g
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c) graphics package d) ggplot2 pack
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In addition to aesthetics, faceting
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Datasets FTIR HPLC e-nose PLS-DA (L
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Figure 6-10 Interactive dendrogram
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6.4 Conclusion The work reported in
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large number of individual models i
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The generated suite of tools, as pr
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In addition, the difficulty to corr
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REFERENCES Almeida, J. A. S., Barbo
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Processing., Proceedings of the 12t
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Clarke, B., Fokoué, E. and Zhang,
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spectroscopy and machine learning",
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Gower, J. C. (1975), "Generalized p
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Jardon, M. (2006), Systems Biology:
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Nicolaou, N., Xu, Y. and Goodacre,
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Shah, A. A., Barthel, D., Lukasiak,
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Vera, G., Jansen, R. and Suppi, R.
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Xu, Y. and Goodacre, R. (2012), "Mu
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